The phrase "assay we explored the" is not correct in written English.
It seems to be a typographical error, possibly intending to say "as we explored the."
Example: "As we explored the ancient ruins, we discovered fascinating artifacts."
Alternatives: "as we examined the" or "while we investigated the."
Using this novel assay, we explored the origin of processive movement in kinesin.
Through bisulfite pyrosequencing assay, we explored the association of P2Y12 gene promoter DNA methylation with clopidogrel resistance.
Using an in vitro Matrigel assay, we explored the possibility that incubation of endothelial cells from different sources with ATP would stimulate cell rearrangements into tube-like networks.
Through molecular docking and dynamics simulation assays, we explored the comparative binding pattern of βTrCP1-WD40 domain with ACV and its phospho-derivatives (ACVMP, ACVDP and ACVTP).
As a step towards determining the biological potential of the top, validated APE1 inhibitors from the profiling assays above, we explored the ability of 6-hydroxy-DL-DOPA, Reactive Blue 2, myricetin, Tyrphostin AG 538, thiolactomycin, methyl 3,4-dephostatin and NSC-13755 to inactivate AP site cleavage activity of protein extracts from HEK 293T and HeLa cells.
As our hospital used a manual pyrogallol red dye-based urine protein assay until 2009, we explored the relationship between urinary creatinine concentrations and (24-hour) PrCr in a cohort of 198 women who had a 24-hour urine collection for protein at our hospital between 1997 and 2004 [ 6].
Here, through comparative structure analysis and molecular dynamics simulation assays, we explored comparative binding pattern of phospho-p68 against β-catenin.
To afford a capacity for concurrent operation of electrophoretic mobility shift assays, we explored fsPAG structures seated on an open planar polymer substrate.
We explored the accuracy of our assay in detecting integer level CNV by analyzing the number of copies of the X-linked gene, G6PD, in DNA samples from patients with known X-chromosome aneuploidy.
Using a systematic series of electrophoretic mobility shift assays (EMSA), we have explored the basis for the sequence-specific DNA-binding by FOXP3.
Using a widely accepted planar migration assay we first explored whether the migratory capabilities of fetal and adult fibroblasts differed either at baseline or in response to growth factors implicated in wound healing.
